Awesome Chemistry Experiments For 135643-82-2

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H14O4, you can also check out more blogs about135643-82-2

Chemistry, like all the natural sciences, begins with the direct observation of nature— in this case, of matter. 135643-82-2, Name is Methyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetate, molecular formula is C8H14O4. In a Article,once mentioned of 135643-82-2, Computed Properties of C8H14O4

Syntheses of 5′-acyl furanosteroids are described from the corresponding unsubstituted [3,2-b]furanosteroids using acid anhydrides and acid chlorides in the presence or absence of Lewis acids. New methods have been developed to prepare 5′-acetyl derivatives: reduction of a 5′-trichloroacetyl intermediate either by sodium formaldehyde sulfoxylate or with 10% Pd/C. Most of these 5′- acyl derivatives bind to the rat ventral prostate androgen receptor. However the antiandrogenic activity was diminished when compared with 4, 5′- methylsulfonyl furanosteroid. Biological studies revealed that 5′-acyl furanosteroids were either androgens or modest antiandrogens. The electrostatic potential maps of the substructures of 3, 4, and 5′-acetyl syn- and anti-furanosteroids showed striking differences which may explain, to some extent, the lack of significant antiandrogenic activity of 5′-acyl furanosteroids.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H14O4, you can also check out more blogs about135643-82-2

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics